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Methanol → HCID 88815335, 화합물

HRID 461677
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HRID 461677 반응식
[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7].[OH:11][P:12]([F:15])([OH:14])=[O:13].O.CO>C(O)C>[P:12]([F:15])([OH:14])([OH:13])=[O:11].[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 887MethanolHCID 962WaterHCID 5962L-LysineHCID 24267Fluorophosphoric acid

생성물 1

HCID 88815335HCID 88815335, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

L-lysine monofluorophosphate was prepared by combining 29.2 grams of free-base lysine with 20 gm. (grams) of monofluorophosphoric acid in about 75 ml. of water. The resulting clear syrupy solution was poured into 750 ml. of a 50:50 mixture of methanol and ethanol (absolute) to precipitate the solid salt. The cake was collected after filtration and rinsed with methanol. The product (L-lysine monofluorophosphate) was then air dried. The L-lysine monofluorophosphate was tested in rat diets as described in Example I but at a level of 6.8 ppm fluoride. Caries reduction was 36%.

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후처리

  1. additionThe resulting clear syrupy solution was poured into 750 ml
  2. customto precipitate the solid salt
  3. customThe cake was collected
  4. filtrationafter filtration
  5. washrinsed with methanol
  6. customair dried

출처 및 근거

ORD 기록
ord-ae0c6452811a4f19bc05971ba169c3d6
출처 데이터셋
uspto-grants-1977_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04064138

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